Triphenylphosphine → 2-(4-[(e)-Hex-2-enyloxy]phenyl)-5-octylthiazole

HRID 2121303Notes

Reaction equation

HRID 2121303 reaction equation
C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.[CH2:20]([OH:26])/[CH:21]=[CH:22]/[CH2:23][CH2:24][CH3:25].O[C:28]1[CH:33]=[CH:32][C:31]([C:34]2[S:35][C:36]([CH2:39][CH2:40][CH2:41][CH2:42][CH2:43][CH2:44][CH2:45][CH3:46])=[CH:37][N:38]=2)=[CH:30][CH:29]=1.CCOC(/N=N/C(OCC)=O)=O>O1CCCC1>[CH2:20]([O:26][C:28]1[CH:33]=[CH:32][C:31]([C:34]2[S:35][C:36]([CH2:39][CH2:40][CH2:41][CH2:42][CH2:43][CH2:44][CH2:45][CH3:46])=[CH:37][N:38]=2)=[CH:30][CH:29]=1)/[CH:21]=[CH:22]/[CH2:23][CH2:24][CH3:25]

Participants

6

Procedure

Triphenylphosphine (0.95 g) is added in small portions to a solution of (E)-hex-2-en-1-ol (0.40 g), 2-(4-hydroxyphenyl)-5-octylthiazole (0.70 g), diethylazodicarboxylate (0.60 g) in dry tetrahydrofuran (40 cm3) at 0° C. under an atmosphere of nitrogen. The reaction mixture is stirred at room temperature overnight. The solvent is removed under reduced pressure and the crude product was purified by column chromatography on silica gel using a 4:1 petroleum (40-60° C.) ether/ethyl acetate mixture as eluent, followed by recrystallisation from ethanol to yield 0.15 g of 2-(4-[(E)-hex-2-enyloxy]phenyl)-5-octyfthiazole.

Workup

  1. customThe solvent is removed under reduced pressure
  2. customthe crude product was purified by column chromatography on silica gel using a 4:1 petroleum (40-60° C.) ether/ethyl acetate mixture as eluent
  3. customfollowed by recrystallisation from ethanol
  4. customto yield 0.15 g of 2-(4-[(E)-hex-2-enyloxy]phenyl)-5-octyfthiazole

Sources & evidence

ORD record
ord-a097de3f9d71474190a55feb879d52ec
Source dataset
uspto-grants-2004_02
Patent number
US06696110B1

Reaction notes

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